KILLIAN NASAL SPECULUM 465-323

GUDID 00192896079618

KILLIAN NASAL SPECULUM WITH FIBER LIGHT GUIDE FIXATION SCREW

SONTEC INSTRUMENTS, INC.

Ear speculum, reusable

• Primary Device ID: 00192896079618
• NIH Device Record Key: 2878ff7a-01aa-4878-b9a9-6269aeb7ee30
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KILLIAN NASAL SPECULUM
• Version Model Number: 465-323
• Catalog Number: 465-323
• Company DUNS: 040729840
• Company Name: SONTEC INSTRUMENTS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Length: 5.25 Inch
• Length: 5.25 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896079618 [Primary]

FDA Product Code

• EPY: SPECULUM, ENT

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00192896079618]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-10-22
• Device Publish Date: 2018-09-20

On-Brand Devices [KILLIAN NASAL SPECULUM]

• 00192896079618: KILLIAN NASAL SPECULUM WITH FIBER LIGHT GUIDE FIXATION SCREW
• 00192896079601: KILLIAN NASAL SPECULUM WITH FIBER LIGHT GUIDE FIXATION SCREW
• 00192896095670: KILLIAN NASAL SPECULUM WITH FIBER OPTIC LIGHT GUIDE FIXED SCREW
• 00192896097872: KILLIAN NASAL SPECULUM WITH FIBER OPTIC LIGHT GUIDE